An adenoviral vector system for functional identification of nuclear receptor ligands

Mol Endocrinol. 1991 Feb;5(2):300-9. doi: 10.1210/mend-5-2-300.

Abstract

A recombinant adenovirus system has been designed that confers glucocorticoid responsiveness upon infected cells in culture. Two mutually dependent viruses are required: a trans-activator virus containing the human glucocorticoid receptor transcription unit and a second receptor virus harboring a glucocorticoid response element linked to the firefly luciferase gene. Another reciprocal pair of viruses has been generated; one member expresses the rat thyroid hormone receptor alpha, while the other contains the luciferase gene regulated by a thyroid hormone-responsive DNA element. Corticosteroid- or thyroid hormone-induced transcription can be efficiently and accurately quantitated from cells coinfected with the appropriate complementary virus pair 20 h after infection in 96-well microtiter plates. This coinfection assay offers a convenient way to measure transcriptional activation by nuclear receptors and has certain key advantages over the commonly used cotransfection method. Its sensitivity and precision make it a practical approach to rapidly identify substances extracted from complex biological samples activating candidate "orphan" nuclear receptor molecules.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae / genetics*
  • Animals
  • Avian Sarcoma Viruses / genetics
  • Cell Line
  • Cell Nucleus / metabolism*
  • Cloning, Molecular
  • DNA, Recombinant
  • Dexamethasone / metabolism
  • Dexamethasone / pharmacology
  • Gene Expression
  • Genetic Vectors*
  • Humans
  • Luciferases / genetics
  • Plasmids
  • Rats
  • Receptors, Cell Surface / metabolism*
  • Receptors, Glucocorticoid / genetics
  • Receptors, Thyroid Hormone / genetics
  • Transcription, Genetic
  • Transfection
  • Triamcinolone Acetonide / metabolism
  • Triamcinolone Acetonide / pharmacology

Substances

  • DNA, Recombinant
  • Receptors, Cell Surface
  • Receptors, Glucocorticoid
  • Receptors, Thyroid Hormone
  • Dexamethasone
  • Luciferases
  • Triamcinolone Acetonide